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Population Genomics of microorganisms and their hosts in health and disease Current Research

Evolutionary genomics of bacteria


The increasing availability of bacterial genomes has opened the possibility for addressing fundamental questions of the evolutionary biology of bacteria:

  1. What does the genome wide variation can tell us about the demographic history of bacterial species?
  2. How has the gene composition of the genomes changed over time?
  3. How has the acquisition of genes (outside of the common drug resistance genes) via lateral gene transfer contributed to the adaptation of bacterial species to new niches?

We have been working on applying some of the recent advances in population genomic techniques to understand the evolutionary history of microbes. An example of the kind of studies we have done revealed that Streptococcus mutans populations, the cavities causing bacteria, have been expanding, most likely after the origin of agriculture. More importantly, we have found that there is a subset of genes, unique to this species, which are functionally involved in the metabolism of sugars and resistance to low pH environments, selective pressures that the bacteria had to face after the change of diet that accompanied the development of agriculture.

In my lab we are interested in applying the same analysis framework to other moderately recombining bacterial species (commensal and pathogenic) to try understand how populations of bacteria have changed in time and how the changes in human population have modified the population demographics of its pathogens and vice versa.

Biology of recombination in bacteria

In bacteria, recombination is a rare event and not part of its reproductive process. Nevertheless, the importance that Horizontal Gene Transfer (HGT in a broad sense) plays in the adaptive evolution of bacteria species is increasingly recognized. Because of its ability to acquire genes and genetic elements from other organisms, the pace of adaptive evolution in bacteria (i.e. invasion of new niches, competition against other bacteria or acquisition of resistance to antibiotics and other environmental stresses) need not to be limited by the amount of standing variation in the population.

But then, we can ask ourselves: why do bacteria maintain an intricate machinery for homologous gene recombination? What is the impact of homologous gene recombination on the maintenance and accessibility of standing genetic variation in populations where sex is not frequent and not linked to reproduction? These are questions that are not well understood.  Our work suggests that, once established in the population, the ability to recombine can be maintained in the population at the expense of its costs.

Nevertheless, because of the frequency and density-dependent nature of horizontal gene transfer in bacteria, the benefits of recombination are not that clear when this ability is rare.  We have performed computational studies to generate testable hypothesis about the evolution of recombination in bacterial populations that we plan on pursuing in the future using Streptococcus pneumoniae as a model system.

 

Another important aspect of recombination in bacteria is understanding the factors that limit or promote the acquisition of foreign DNA into the cell. My previous work, done in collaboration with Daniel Rozen (now at the University of Leiden, the Netherlands) has shown that, contrary to some hypothesis proposed in the microbial molecular genetics literature, the polymorphism in the competence system responsible for inducing the uptake of DNA does not maintain genetically differentiated populations. This research has also open the door to interesting findings on the evolution of the polymorphism of two component systems (receptor – signal peptides) and we plan on pursuing additional experimental work to understand how polymorphism can be maintained by purifying selection via compensatory mutations.  The interesting bit is that while sequence-wise the competence system presents strong similarities with self-compatibility systems in plants, the mechanisms maintaining polymorphism in the population are radically different.

Additional work performed by Benjamin Evans, a former student of Danny Rozen has shown results that are consistent with our original assessment of the impact of the polymorphism on the population substructure of S. pneumoniae.

Ecology and evolution of bacteriocins

Agents that kill the organisms that produce them or other, genetically identical members of their populations are intriguing puzzles for ecologists and evolutionary biologists. How can such “self-killing” agents, which, on a first consideration appear to be a considerable disadvantage to the organisms that produce them evolve and be maintained by natural selection?  One possibility we have suggested is that these agents can be maintained if during the interaction of different bacterial populations or species, the producing species kill their competitors more than they kill themselves.

This work, at the intersection of experiments and mathematical modeling has also opened the door for an interesting hypothesis about the maintenance of self-killing agents with a set of testable hypotheses: if the toxin producing bacterium kills others more than it kills itself, then such a system could potentially be maintained. Nevertheless, as with the advantage of recombination, this mechanism engenders a cost to the organism and its action is frequency or density-dependent, making the question of its origin and maintenance very controversial.

 

 

Relevant publications